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Merck
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W285609

Sigma-Aldrich

α-水芹烯

≥75%, stabilized

别名:

2-甲基-5-（1-甲基乙基）-1，3-环己二烯

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About This Item

经验公式（希尔记法）:
C10H16
CAS号:
99-83-2
分子量:
136.23
FEMA编号:
2856
EC 号:
202-792-5
欧洲委员会编号:
2117
MDL编号:
MFCD00040419
UNSPSC代码:
12164502
PubChem化学物质编号:
24901345
Flavis编号:
1.006
NACRES:
NA.21

生物来源

synthetic

质量水平

400

等级

Halal
Kosher

管理合规性

FDA 21 CFR 172.515

方案

≥75%

旋光性

[α]20/D −139 to −110°, neat

包含

alpha-tocopherol as additive

折射率

n20/D 1.474 (lit.)

密度

0.85 g/mL at 25 °C (lit.)

应用

flavors and fragrances

文件

see Safety & Documentation for available documents

食品过敏原

no known allergens

性状检查

spicy; woody

SMILES字符串

CC(C)C1CC=C(C)C=C1

InChI

1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4-6,8,10H,7H2,1-3H3

InChI key

OGLDWXZKYODSOB-UHFFFAOYSA-N

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应用


  • 绿色意味着清洁吗？常规清洁产品与绿色清洁产品的挥发性有机物排放研究。：研究比较了常规清洁产品和绿色清洁产品中的挥发性有机化合物（VOC）排放，确定a-水芹烯是一种常见成分。研究结果强调了绿色产品的环境影响及其有效性（Harding-Smith et al., 2024）。

  • 基于RNA-Seq的转录组学和GC-MS定量分析的黄皮种子精油抗白色念珠菌机制研究。：研究使用RNA-Seq和GC-MS研究含有a-水芹烯的黄皮精油对白色念珠菌的抗真菌特性，为其潜在的治疗应用提供见解（Ma et al., 2023）。

  • 马钱精油抗霍乱和糖尿病肾保护活性化合物研究：计算和分子动力学研究。本研究确定a-水芹烯是马钱精油中具有抗霍乱和肾脏保护作用的活性化合物，表明其具有治疗霍乱和预防糖尿病肾损伤的潜力（Dahab et al., 2023）。

  • 云斑天牛对黄连木挥发性物质的电生理和行为反应。：研究考察了云斑天牛对来自黄连木的a-水芹烯等挥发性物质的反应。这些发现对使用天然挥发物的病虫害管理策略具有启示意义（Fan et al., 2023）。

免责声明

仅供R&D或非EU食品使用不用于零售。

象形图

FlameHealth hazard
GHS02,GHS08

警示用语：

Danger

危险声明

H226,H304

危险分类

Asp. Tox. 1 - Flam. Liq. 3

储存分类代码

3 - Flammable liquids

WGK

WGK 2

闪点(°F)

116.6 °F - closed cup

闪点(°C)

47 °C - closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
STBK0674
STBJ8194
STBJ5494
STBJ0238
STBH3029

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β-石竹烯 ≥80%, FCC, FG

Sigma-Aldrich

W225207

β-石竹烯

月桂烯 analytical standard

Supelco

64643

月桂烯

α-蒎烯 98%

Sigma-Aldrich

147524

α-蒎烯

马来酸酐 puriss., ≥99.0% (NT)

Sigma-Aldrich

63200

马来酸酐

α-松油烯 analytical standard

Supelco

95652

α-松油烯

桧烯 phyproof® Reference Substance

PHL82342

桧烯

β-Pinene phyproof® Reference Substance

PHL89335

β-Pinene

月桂烯 technical grade

Sigma-Aldrich

M100005

月桂烯

Huai-sheng Hu et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 32(1), 67-70 (2009-05-19)
The chemical constituents and antimicrobial activity of the essential oil from Acanthopanax brachypus were studied. The essential oil was extracted from the stem of A. brachypus by steam distillation, and its antimicrobial activity was tested in vitro. The chemical constituents
M Miyazawa et al.
Journal of agricultural and food chemistry, 48(7), 2893-2895 (2000-07-18)
gamma-Terpinene was mixed in artificial diet at a concentration of 1 mg/g of diet, and the diet was fed to the last instar larvae of common cutworm (Spodoptera litura). Metabolites were recovered from frass and analyzed spectroscopically. gamma-Terpinene was transformed
Gökalp İşcan et al.
Chemistry & biodiversity, 9(8), 1525-1532 (2012-08-18)
Terpene derivatives converted by microbial biotransformation constitute an important resource for natural pharmaceutical, fragrance, and aroma substances. In the present study, the monoterpene α-phellandrene was biotransformed by 16 different strains of microorganisms (bacteria, fungi, and yeasts). The transformation metabolites were
David F Lima et al.
The Journal of pharmacy and pharmacology, 64(2), 283-292 (2012-01-10)
The aim of this work was to investigate the antinociceptive property of α-phellandrene (α-PHE) in experimental nociception models and possible mechanisms involved. Mass spectrometry was used to evaluate the purity and molecular mass of α-PHE. Macrophages from mice peritoneal cavity
S Foss et al.
Systematic and applied microbiology, 21(2), 237-244 (1998-08-15)
Four pseudomonad strains 51Men, 54Pin, 62Car and 65Phen were recently isolated on the monoterpenes (+)-menthene, alpha-pinene, 2-carene and alpha-phellandrene as sole carbon source and nitrate as electron acceptor. These bacteria were characterised. The motile, mesophilic, Gram-negative rods had a strictly
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实验方案

Sweet Orange Essential Oil GC Analysis

Fast GC analysis of sweet orange essential oil in hexane. Key components identified includes: β-Farnesene; α-Huµlene; Germacrene D; (+)-Valencene; Bicyclogermacrene; (+)-δ-Cadinene

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